Allele Registry

Canonical Allele Identifier: PA2826464504

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000213657

RCV002514351

RCV003452845

ClinVar Variation:

90715

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr486Pro	CA018802 NM_001258281.1:c.1456A>C